Section 03 · Monograph

Midodrine

Reviewed Nov 2026FDA label
ProAmatineAlpha-1 agonist
Forms
Tab: 2.5, 5, 10mg
Dose
2.5-10mg TID daytime (last dose at least 4h before bed)
MOA
Peripheral vasoconstriction (orthostatic hTN)

Black Box Warning

  • Can cause marked elevation of supine blood pressure; use only in patients whose lives are considerably impaired despite standard care, and continue only if clinical benefit is documented

Indications

  • Symptomatic orthostatic hypotensionFDA-labeled

Mechanism of Action

  • Prodrug converted to desglymidodrine, a selective alpha-1 agonist causing arteriolar and venous vasoconstriction and raising standing blood pressure

Full Dosing

Adult / usual

  • Start 2.5mg three times daily; titrate (commonly up to 10mg TID) as tolerated
  • Give during daytime upright hours — morning, midday and late afternoon; last dose at least 4 hours before bedtime

Renal

  • Renal impairment: start at 2.5mg

Contraindications

  • Severe organic heart disease
  • Acute renal disease
  • Urinary retention
  • Pheochromocytoma or thyrotoxicosis
  • Persistent and excessive supine hypertension

Drug Interactions

  • Other vasoconstrictors: additive pressor effect
  • Digoxin and beta-blockers: bradycardia and AV block
  • Fludrocortisone: additive effect on supine hypertension

Adverse Effects

  • Supine hypertension
  • Piloerection (goosebumps), scalp pruritus or tingling
  • Urinary retention
  • Bradycardia

Monitoring Parameters

  • Supine and standing blood pressure
  • Urinary symptoms
  • Renal function

Pregnancy & Lactation

  • Limited data; use only if benefit justifies risk
  • Unknown whether present in milk

References

  1. Midodrine Prescribing Information — DailyMed (NIH) search